510(k) K842503 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass
GAMBRO PULSATILE MONITOR PLM 10-200
| Applicant | Gambro, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 10, 1984 |
| Received | Jun 26, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842503
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.